Question 5 Please predict the products for each of the following reactions: 1. Na 2. PrBr Na 10 1. TsCl, Py 2. NaBr, DMSO SOCI₂, Py H-NO CrO3Cl TsCl y (pyridine) Py ( PCC OH Na2Cr2O7 H2SO4 HCI ZnCl2 2. KI, DMF 1. MsCI, Et3N (base) A B C D А ABCD OMS NO REACTION
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- Question 3 Please predict the products for each of the following reactions: Na 1. Na 2. PrBr 1. TsCl, Py 2. NaBr, DMSO SOCI₂, Py 9 10 H-NO Cro₂Cl TsCl Py (pyridine) 3 OH 5 PCC Na2Cr2O7 H2SO4 HCI ZnCl2 1. MsCI, Et N (base) 2. KI, DMF A B с D ABCD H OH NO REACTIONQuestion 8 Please predict the products for each of the following reactions: ABCD A 1. Na 2. PrBr Na 10 1. TsCI, Py 2. NaBr, DMSO SOCI₂, Py H-NG Cro₂Cl Py (pyridine) OH PCC Na2Cr2O7 H2SO4 HCI ZnCl2 1. MsCI, Et N (base) 2. KI, DMF B с D BrChemist Escoja los reactivos necesarios para la siguiente síntesis: A Br OH A = Mg, THF B = PCC, CH2C12 C= 1. acetona; 2. H2O Leyenda de reactivos: acetona = O + x + x formaldehido= H H MgBr B OH acetaldehído= H
- Please predict the products for each of the following reactions: A Na 2. PrBr 1. Na 1. TsCI, Py 2. NaBr, DMSO SOCI₂, Py B 9 8 10 H-NO CrO₂Cl TSCI Py (pyridine) OH 3 1. MSCI, Et3N (base) 2. KI, DMF C PCC NO REACTION Na₂Cr₂O7 H₂SO4 HCI ZnCl₂ D OHQuestion 4 Please predict the products for each of the following reactions: Na 1. Na 2. PrBr TsCl Py (pyridine) 1. TsCl, Py 2. NaBr, DMSO 9 10 SOCI₂, Py H-N→ CrO3Cl PCC OH Na2Cr2O7 H2SO4 5 HCI ZnCl2 2. KI, DMF 1. MsCI, Et₂N (base) A B C A C (BUD NO REACTION DQuestion 4 Please predict the products for each of the following reactions: 1. Na 2. PrBr Na 10 1. TsCl, Py 2. NaBr, DMSO SOCI₂, Py H-N→ Θ Cro₂Cl TsCl Py (pyridine) OH PCC Na2Cr2O7 H2SO4 HCI ZnCl2 1. MsCI, Et N (base) 2. KI, DMF A B с ABCD NO REACTION D
- 16 What is X in the following reaction? * (i) X CH,-C=C-CH, (ii) H+/Zn CH,-C-C-CH, HNO3 02 03 KMN04 None of the above0 The target diol is synthesized in one step from 1-methylcyclopentene, but your lab partner exhausted the supply of that alkene. Fortunately, you have plenty of isomers (CH₁) on hand from which to synthesize 1-methylcyclopentene and, ultimately, the diol. Provide the missing reagents and organic structures needed to most efficiently produce the target product. reagent 1 Compound A Draw compound A. Select Draw Rings More с H Compound B Erase reagent 2 Identify reagent 1. reagent 3 H3C.. HO ....|H OHH14.41 - Level 3 :: Unanswered • 3 attempts left Compound A produces compound E in four steps. What is compound A? a b C C D d E e Br 1) MeMgBr H2Cr207 1) MgBr H2SO4 (conc.) 2) H20 2) H2O NaBr Possible starting materials HO H. HO. a) b) c) d) e) A
- Question 9 Please predict the products for each of the following reactions: A ABCD 1. Na 2. PrBr เวรเ Py (pyridine) Na 10 9 OH 18 1. TsCI, Py 2. NaBr, DMSO SOCI₂, Py H-N'+ CrO3Cl PCC Na2Cr2O7 H2SO4 HCI ZnCl2 2. KI, DMF 1. MsCI, Et N (base) B с D Na NO REACTIONWhat is the major organic product of the following reaction? Problem viewing the image, Click Here O A OB O C OD A. B. C. C. D. 1. Hg(OAc)2, H₂O 2. NaBH4 D. OH t to allo OH OH f OH (+) OH (+) (±)envellum.ecollege.com/course.html?courseld%3D16785381&OpenVellumHMAC=D7ff12f8acf82e26893816a5833de5626#310001 SHOmewOrK #4 Problem 12 12 of Propose a mecnanism or ihe following reaction: CH3 CH3 H20 HQ CH3 H* CH3 Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. Electron flow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new should be created. H EXP. . ? CONT. CH CH, +) H. Pearson 8:29 )耳. @ here to search 73°F 23 10/3/ DELL